We routinely culture H1 cells as colonies on matrigel, in mTESR1. We usually split with dispase for stock maintenance or with Versene-EDTA for transfecting plasmids. We get a 20-30% transfection efficiency of DNA which is still enough to create clones but been so fan unable to silence by siRNAs even though I have tried more than 10 different lipids. 

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